Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48587346T>A , CM000681.2:g.48587346T>A | GRCh38 |
| NC_000019.9:g.49090603T>A , CM000681.1:g.49090603T>A | GRCh37 |
| NC_000019.8:g.53782415T>A | NCBI36 |
| NG_029063.1:g.40175T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000201586.7:c.332T>A MANE Select | ENSP00000201586.2:p.Phe111Tyr | |
| ENST00000201586.6:c.332T>A | ENSP00000201586.1:p.Phe111Tyr | |
| ENST00000323090.4:c.287T>A | ENSP00000312880.3:p.Phe96Tyr | |
| NM_004605.2:c.287T>A | NP_004596.2:p.Phe96Tyr | |
| NM_177973.1:c.332T>A | NP_814444.1:p.Phe111Tyr | |
| NM_177973.2:c.332T>A MANE Select | NP_814444.1:p.Phe111Tyr |